Phase 2 Pancreatic Cancer Trial, Recruiting NCT06844422 Sponsor: Shandong Cancer Hospital and Institute Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT06844422
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People with locally advanced pancreatic cancer that cannot be removed by surgery, confirmed by a tissue or cell sample test, as classified by a standard medical staging system
  • People aged between 18 and 80 years
  • People who have at least one pancreatic cancer lesion that can be measured using standard imaging criteria
  • People with a good general level of physical functioning, rated 0 or 1 on a standard medical scale (meaning able to carry out normal daily activities with little or no restriction)
  • People with a life expectancy of at least 3 months
  • People whose blood counts, kidney function, and liver function fall within acceptable ranges on tests taken within 14 days before joining (confirm specific values with trial site)
  • People who are able to provide tissue and blood samples for research purposes
  • People who are able to understand the study details and sign a written consent form

Who may not be able to join:

  • People who have had any other cancer in the past 5 years, except for certain localised cancers that have been fully treated and cured
  • People with uncontrolled infections (such as active tuberculosis or hepatitis), uncontrolled whole-body illnesses, poorly controlled high blood pressure or diabetes, or serious health events in the past 6 months such as a heart attack, stroke, or significant heart rhythm problems
  • People who have previously been treated with certain drugs that target specific parts of the immune system's T-cell response (confirm with trial site)
  • People who have received radiation therapy within 2 weeks before joining the trial
  • People with a known allergy to the study drug Ivonescimab or any of its ingredients
  • People who are pregnant or currently breastfeeding
  • People who are currently using or planning to use certain medications that strongly affect how the body processes drugs (known as strong CYP3A4/5 or CYP1A2 inducers or inhibitors — confirm specific medications with trial site)
  • People who require certain blood-thinning tablets called oral vitamin K antagonists (such as full-dose warfarin), though low-dose warfarin and some other low-dose blood thinners may be permitted (confirm with trial site)
  • People who have conditions that affect their ability to take oral medications, including a history of a hole or abnormal opening in the gut in the past 6 months, bowel obstruction, large bowel surgery, Crohn's disease, ulcerative colitis, or ongoing chronic diarrhoea

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Jinbo Yue, Doctor, Shandong Cancer Hospital and Institute

Phone: 0531-67626442

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Shandong Cancer Hospital and Institute
Registry
ClinicalTrials.gov
Start date
8 February 2025
Est. completion
18 February 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Maximum Tolerated Dose (MTD); Dose-Limiting Toxicity (DLT); Recommended Phase 2 Dose (RP2D); Progression-Free Survival (PFS)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov